Canonical Allele Identifier: CA1142935299

Gene: ARID1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26779209C= , CM000663.2:g.26779209C=	GRCh38
NC_000001.10:g.27105700C= , CM000663.1:g.27105700C=	GRCh37
NC_000001.9:g.26978287C=	NCBI36
NG_029965.1:g.88179C= , LRG_875:g.88179C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.5311C= MANE Select	ENSP00000320485.7:p.Pro1771=
ENST00000374152.7:c.4162C=	ENSP00000363267.2:p.Pro1388=
ENST00000430799.7:c.4159C=	ENSP00000390317.3:p.Pro1387=
ENST00000466382.2:c.728C=
ENST00000636219.1:c.4165C=	ENSP00000489842.1:p.Pro1389=
ENST00000637788.1:n.1111C=
ENST00000324856.11:c.5311C=	ENSP00000320485.7:p.Pro1771=
ENST00000374152.6:c.4162C=	ENSP00000363267.2:p.Pro1388=
ENST00000430799.6:c.2000C=
ENST00000457599.6:c.4660C=	ENSP00000387636.2:p.Pro1554=
ENST00000466382.1:c.728C=
ENST00000532781.1:c.809C=
NM_006015.4:c.5311C= , LRG_875t1:c.5311C=	NP_006006.3:p.Pro1771=
NM_139135.2:c.4660C=	NP_624361.1:p.Pro1554=
NM_006015.5:c.5311C=	NP_006006.3:p.Pro1771=
NM_139135.3:c.4660C=	NP_624361.1:p.Pro1554=
NM_006015.6:c.5311C= MANE Select	NP_006006.3:p.Pro1771=
NM_139135.4:c.4660C=	NP_624361.1:p.Pro1554=